Recall of Nasopharyngeal sample collection trays for COVID-19 testing due to potential improper assembly by untrained individuals. Affected units include specific model numbers and lots.
Affected products were assembled off-site by individuals who may not have been properly trained.
American Contract Systems is recalling certain Nasopharyngeal sample collection trays used for COVID-19 testing because they may have been assembled by individuals without proper training. This could lead to improper use of the trays during testing procedures.
The trays were assembled off-site by individuals who may not have been properly trained. This could result in improper use during COVID-19 testing procedures, potentially affecting the accuracy or safety of the samples collected.
Healthcare workers and individuals using these trays for COVID-19 testing are likely affected. Those handling the specific model numbers and lots listed in the recall are at the highest risk.
Check for the model label 'COVID TEST KIT NONSTERILE 184312, AHCV18A' and lot numbers 721211, 672211, 657211, 994221, 980221, or 974221 on the tray.
Identify the model label and lot numbers to confirm if your tray is affected.
The product was assembled off-site by individuals who may not have been properly trained, which could lead to improper use during COVID-19 testing.
Affected model: COVID TEST KIT NONSTERILE 184312, AHCV18A. Affected lots: 721211, 672211, 657211, 994221, 980221, 974221.
The recall does not specify a remedy, so check the product details to see if it is affected and contact the manufacturer if needed.
We’ve drafted a message you can send American Contract Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1277-2022 — American Contract Systems American Contract Systems Hello, I own a American Contract Systems that is covered by recall Z-1277-2022 from American Contract Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
